methyl (1R,2S,4aR,4bS,5S,6aS,9R,10R,10aS,12aS)-5,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate

Details

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Internal ID bbfd8694-e105-49aa-b901-318334546c63
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids > 16-oxosteroids
IUPAC Name methyl (1R,2S,4aR,4bS,5S,6aS,9R,10R,10aS,12aS)-5,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate
SMILES (Canonical) CC1CCC2(CC(C3(C(=CCC4C3(CCC(C4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)C2C1(C)O)C)O)C(=O)OC
SMILES (Isomeric) C[C@@H]1CC[C@@]2(C[C@@H]([C@@]3(C(=CC[C@@H]4[C@]3(CC[C@@H]([C@]4(C)CC(=O)OC)C(C)(C)C(=O)OC)C)[C@@H]2[C@]1(C)O)C)O)C(=O)OC
InChI InChI=1S/C33H52O8/c1-19-13-16-33(27(37)41-10)17-23(34)31(6)20(25(33)32(19,7)38)11-12-22-29(4,18-24(35)39-8)21(14-15-30(22,31)5)28(2,3)26(36)40-9/h11,19,21-23,25,34,38H,12-18H2,1-10H3/t19-,21-,22+,23+,25-,29+,30-,31+,32-,33+/m1/s1
InChI Key HFBJCUAOHBIRFA-STGPNOLNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H52O8
Molecular Weight 576.80 g/mol
Exact Mass 576.36621861 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.85
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1R,2S,4aR,4bS,5S,6aS,9R,10R,10aS,12aS)-5,10-dihydroxy-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 - 0.7024 70.24%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8900 89.00%
OATP2B1 inhibitior - 0.7192 71.92%
OATP1B1 inhibitior + 0.8596 85.96%
OATP1B3 inhibitior - 0.4768 47.68%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9462 94.62%
P-glycoprotein inhibitior + 0.7138 71.38%
P-glycoprotein substrate + 0.5521 55.21%
CYP3A4 substrate + 0.6977 69.77%
CYP2C9 substrate - 0.8108 81.08%
CYP2D6 substrate - 0.8629 86.29%
CYP3A4 inhibition - 0.7107 71.07%
CYP2C9 inhibition - 0.8332 83.32%
CYP2C19 inhibition - 0.9094 90.94%
CYP2D6 inhibition - 0.9466 94.66%
CYP1A2 inhibition - 0.8875 88.75%
CYP2C8 inhibition + 0.5724 57.24%
CYP inhibitory promiscuity - 0.8858 88.58%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9743 97.43%
Carcinogenicity (trinary) Non-required 0.7358 73.58%
Eye corrosion - 0.9941 99.41%
Eye irritation - 0.9194 91.94%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.7698 76.98%
Human Ether-a-go-go-Related Gene inhibition - 0.5178 51.78%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5815 58.15%
skin sensitisation - 0.6900 69.00%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.5825 58.25%
Acute Oral Toxicity (c) III 0.7475 74.75%
Estrogen receptor binding + 0.6528 65.28%
Androgen receptor binding + 0.7235 72.35%
Thyroid receptor binding + 0.5610 56.10%
Glucocorticoid receptor binding + 0.7790 77.90%
Aromatase binding + 0.7294 72.94%
PPAR gamma + 0.6397 63.97%
Honey bee toxicity - 0.7489 74.89%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9957 99.57%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.91% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.71% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.49% 96.09%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 93.64% 91.07%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.87% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.14% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.64% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.49% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.90% 97.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.46% 89.34%
CHEMBL1871 P10275 Androgen Receptor 82.94% 96.43%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.80% 93.03%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.76% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.55% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.37% 97.14%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.26% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.04% 82.69%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.34% 96.90%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.54% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.40% 96.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.34% 94.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Musanga cecropioides

Cross-Links

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PubChem 162884196
LOTUS LTS0121426
wikiData Q105027216